Two Cases of Hallermann-Streiff Syndrome with Retinal Abnormalities

dc.contributor.author	Maka Erika
dc.contributor.author	Lukáts Olga
dc.contributor.author	Bausz Mária
dc.contributor.author	Nagy Zoltán Zsolt
dc.contributor.author	Resch Miklós
dc.date.accessioned	2018-05-01T10:59:40Z
dc.date.available	2018-05-01T10:59:40Z
dc.date.issued	2015
dc.identifier.citation	pagination=1000424; journalVolume=6; journalIssueNumber=2; journalTitle=JOURNAL OF CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY;
dc.identifier.uri	http://repo.lib.semmelweis.hu//handle/123456789/5319
dc.identifier.uri	doi:10.4172/2155-9570.1000424
dc.description.abstract	Hallermann-Streiff syndrome is a rare congenital disorder that is characterized by malformations of the craniofacial region with ocular abnormalities. Some ophthalmic signs can be observed in early age and some in adulthood. The visual functions are determined by a lot of factors including microphthalmos, cataract and fundus abnormalities. We report two cases of Hallermann-Streiff syndrome identified in our department in the last decade.
dc.title	Two Cases of Hallermann-Streiff Syndrome with Retinal Abnormalities
dc.type	Journal Article
dc.date.updated	2018-05-01T07:21:32Z
dc.language.rfc3066	en
dc.identifier.mtmt	2959015
dc.contributor.department	SE/AOK/K/Szemészeti Klinika
dc.contributor.institution	Semmelweis Egyetem